2-Iodo-6-nitrophenol

Base Information

• Chemical Name: 2-Iodo-6-nitrophenol
• CAS No.: 13073-26-2
• Molecular Formula: C6H4INO3
• Molecular Weight: 265.007
• Hs Code.: 2908990000
• European Community (EC) Number: 970-793-4
• DSSTox Substance ID: DTXSID00544393
• Nikkaji Number: J707.361E
• Wikidata: Q82421496
• Mol file: 13073-26-2.mol

Synonyms:2-Iodo-6-nitrophenol;13073-26-2;2-iodo-6-nitro-phenol;Phenol, 2-iodo-6-nitro-;6-iodo-2-nitrophenol;SCHEMBL7114571;DTXSID00544393;MFCD00859244;AKOS022172087;PS-10599;CS-0148052;D92861

Chemical Property of 2-Iodo-6-nitrophenol

Chemical Property:

• Melting Point: 110 °C
• Boiling Point: 229.2±20.0 °C(Predicted)
• PKA: 5.46±0.24(Predicted)
• PSA: 66.05000
• Density: 2.176±0.06 g/cm3(Predicted)
• LogP: 2.42820
• Storage Temp.: 2-8°C
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 264.92359
• Heavy Atom Count: 11
• Complexity: 158

Purity/Quality:

95% ^*data from raw suppliers

2-iodo-6-nitrophenol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC(=C(C(=C1)I)O)[N+](=O)[O-]

Technology Process of 2-Iodo-6-nitrophenol

There total 20 articles about 2-Iodo-6-nitrophenol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

2-hydroxynitrobenzene (88-75-5,78813-12-4) → 4-iodo-2-nitrophenol (21784-73-6) + 2-iodo-6-nitro-phenol (13073-26-2)

Guidance literature:

With Oxone; potassium iodide; In methanol; at 20 ℃; for 48h;

DOI:10.1081/SCC-120006002

Reference yield: 1.0%

thallium(I) 2-nitrophenoxide (32707-02-1) → 4-iodo-2-nitrophenol (21784-73-6) + 2-iodo-6-nitro-phenol (13073-26-2) + 2-hydroxynitrobenzene (88-75-5,78813-12-4)

Guidance literature:

With iodine; In dichloromethane; for 24h; Ambient temperature;

DOI:10.1071/c97051

Reference yield:

2,6-diiodo-phenol (28177-54-0) → 2,6-diiodo-4-nitrophenol (305-85-1) + 2-iodo-6-nitro-phenol (13073-26-2)

Guidance literature:

With nitric acid;

upstream raw materials:

2-Iodophenol

2,6-diiodo-phenol

acetic acid

benzene

Downstream raw materials:

6-iodo-2,4-dinitrophenol

diiodo-4,6 nitro-2 phenol

2-iodo-6-nitro-anisole

2,4,6-Trinitrophenol